Clinical Research Associate I/ Clinical Research Associate II

Precision for Medicine

Turkey

On-site

TRY 894,054 - 2,235,136

Full time

14 days+
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Job summary

A leading clinical research organization is seeking a Clinical Research Associate I / II in Turkey to monitor and oversee clinical studies. This position offers the ability to work fully remotely while focusing on a manageable number of studies to ensure high quality and impact. The ideal candidate will possess a relevant university degree and at least 6 months of CRA experience. Fluency in English and Turkish is essential, along with excellent communication and organizational skills. Up to 60% travel may be required.

Qualifications

  • At least 6 months of experience as a CRA in CRO or pharmaceutical industry.
  • Oncology monitoring experience required.
  • Site management experience in clinical research.

Responsibilities

  • Monitor and own the progress of clinical studies at investigative sites.
  • Ensure clinical studies are conducted according to protocol and regulations.
  • Coordinate activities to set up and monitor studies.

Skills

Excellent communication skills
Organizational skills
Client-focused approach
Team player
Fluency in English
Fluency in Turkish

Education

University degree in life science, pharmacy or health-related discipline

Tools

Computerized information systems
Electronic spreadsheets
Word processing software
Electronic mail

Job description

Clinical Research Associate I / Clinical Research Associate II

Remote, Turkey.

Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully – your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

Precision for Medicine is recruiting Clinical Research Associate I / Clinical Research Associate II to join our team in Turkey. This position can be offered fully home based.

About You
  • You are calm, thoughtful, and responsive when things don’t go as planned.
  • You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
  • You find quick and creative ways of overcoming difficulties.
  • You have an impeccable eye for detail.
  • You identify potential study risks and propose solutions on how to mitigate them.
  • You take responsibility in the quality and outcomes of your work.
  • You are adept at handling conflict by using tried and true resolution strategies.
Responsibilities

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH‑GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; help prepare regulatory submissions, conduct pre-study and initiation visits, etc.).

Qualifications
Minimum Requirements
  • University degree in life science/pharmacy/other health‑related discipline or equivalent experience in a scientific or healthcare discipline or be a licensed health care professional.
  • At least 6 months of experience as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management experience or equivalent experience in clinical research.
  • Oncology monitoring experience.
Other Requirements
  • Excellent communication and organizational skills are essential. A team player.
  • Evidence of a client‑focused approach.
  • Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required.
  • Ability to travel overnight. Up to 60% travel on average, based on regional requirements. International travel as needed.
  • Fluency in English and Turkish.
Preferred
  • Startup activities experience.
Equal Opportunity

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.

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